This retrospective study was conducted at the Infectious Diarrhea Clinic of Peking University Third Hospital, a large grade A tertiary care hospital located in Haidian District, Beijing. The clinic serves a diverse population, including local residents, university students from surrounding academic institutions, and referred patients from the community. It functions as a primary and a secondary care access point, as well as a tertiary referral center. Data were collected from patients treated for foodborne diseases during two periods: January 2018 to December 2019 (group A, prepandemic) and January 2022 to December 2023 (group B, postpandemic).

The years 2020 and 2021 were excluded from the analysis because they represent the peak of the COVID-19 pandemic in Beijing, during which routine infectious diarrhea clinic services were substantially disrupted, surveillance protocols were altered, and patient care-seeking patterns were profoundly affected. We acknowledge that excluding this period creates a discontinuity in the temporal trends and limits our ability to capture changes during the most intense phase of the pandemic; however, data from this interval were considered unreliable for comparative analysis because of these major disruptions.

Inclusion criteria were patients aged 16 years or older presenting to the Infectious Diarrhea Clinic and having illness onset associated with food intake or suspected food intake, accompanied by gastrointestinal symptoms, including nausea, vomiting, abdominal pain, and diarrhea.

Exclusion criteria were patients with gastrointestinal diseases clearly diagnosed as nonfoodborne. This study focused exclusively on bacterial and viral foodborne pathogens; nonmicrobial foodborne illnesses, such as those caused by chemical contamination, naturally occurring toxins, or food allergies, were not included in the etiological testing panel and therefore are not represented in these results.

For patients visiting the Infectious Diarrhea Clinic, demographic information (name, age, occupation), clinical symptoms (abdominal pain, diarrhea, fever, fatigue), suspected food exposure history, and stool specimens were collected. Specimens were sent weekly to the Haidian District Center for Disease Control and Prevention for testing, with results reviewed by the Beijing Center for Disease Control and Prevention. Importantly, the diagnostic methods, laboratory protocols, specimen collection procedures, reagent kits, instrumentation, and testing criteria remained unchanged throughout the study period (2018‐2023), with no modifications made to the pathogen testing panel or definitions of positive results.

Laboratory analyses followed the National Foodborne Pathogen Monitoring Manual for isolation, culture, and identification (2015‐2019). Initial screening involved streaking specimens onto agar plates with 24-hour incubation. For positive screens, 5 suspicious diarrheagenic Escherichia coli (DEC) colonies were selected and subjected to biochemical identification using a VITEK2 Compact30 automated system (bioMérieux Inc).

The 5 target pathogens monitored were Salmonella, Shigella, Vibrio parahaemolyticus, DEC, and Norovirus. A specimen was considered etiologically positive if at least 1 of these 5 pathogens was detected. The positivity rate was calculated as the number of positive specimens divided by the total number of patients whose stool specimens were collected and submitted for testing.

This study was approved by the Medical Scientific Research Ethics Committee of Peking University Third Hospital (2024 Medical Ethics Review number 203‐01). All study participants provided informed consent. The study was conducted in accordance with the Declaration of Helsinki.

Data were organized and summarized using Microsoft Excel. Statistical analyses were performed using SPSS version 26.0 for Mac (SPSS Inc). Cases were divided into 2 groups: group A (2018‐2019) and group B (2022‐2023). Age was compared between groups using independent-samples t tests. Qualitative data were expressed as numbers (percentages), and 95% CIs were calculated for key proportions. Group comparisons were made using χ² tests, with P<.05 considered statistically significant.

From January 2018 to December 2019 and from January 2022 to December 2023, a total of 1064 cases meeting the inclusion criteria were seen at the Infectious Diarrhea Clinic. Among them, 561 (52.7%) were male and 503 (47.3%) were female. The predominant age group was 26 to 45 years (n=479, 45%). The top 3 occupations were students (n=377, 35.4%), civil servants (n=284, 26.7%), and retired personnel (n=101, 9.5%). Table 1 presents a comparison of the demographic and occupational characteristics of groups A and B. Clinical symptoms among the cases are summarized in Table 2. The digestive system was the most commonly affected system in both groups (group A: 554/561, 98.8%; group B: 496/503, 98.6%). General symptoms were significantly more frequent in the prepandemic group (group A: 176/561, 31.4%; group B: 62/503, 12.3%; P<.001), while respiratory, cardiovascular/cerebrovascular, urinary, and nervous system symptoms were rare in both groups.

Table 3 shows that mixed foods accounted for the highest proportion in both groups, followed by meat and meat products. χ² tests revealed statistically significant differences between the 2 groups in the proportions of cases associated with vegetables and their products, grains and their products, and other foods (P<.05). The number of cases related to vegetables and their products decreased from 79 to 41 in the postpandemic period, while cases related to grains and their products increased from 24 to 47, and those related to other foods increased from 56 to 70.

Figure 1 compares the number of positive cases for each of the 5 monitored pathogens between the 2 periods. The overall pathogen positivity rate among all tested patients was 22.3% (237/1064). Group A had a positivity rate of 27.6% (155/561, 95% CI 23.9%‐31.3%), which was significantly higher than the 16.3% (82/503, 95% CI 13.1%‐19.5%) observed in group B (P<.05). Annual surveillance data showed the following results: 2018 (228 tested, 65 positive), 2019 (333 tested, 90 positive), 2022 (259 tested, 24 positive), and 2023 (244 tested, 58 positive).

Five pathogens were monitored: Salmonella, Shigella, V parahaemolyticus, DEC, and Norovirus. No Shigella cases were detected in either group. The detection rate of V parahaemolyticus among all tested patients was significantly lower in group B (7/503, 1.4%) than in group A (24/561, 4.3%) (P=.005). No statistically significant differences were observed for Salmonella (group A: 22/561, 3.9%; group B: 13/503, 2.6%) or DEC (group A: 66/561, 11.8%; group B: 45/503, 9%). The detection rate of Norovirus was significantly lower in group B (17/503, 3.4%) than in group A (43/561, 7.7%) (P=.002) (Table 4).

Stacked bar charts show the number of positive cases for each of the 5 monitored pathogens in group A (2018‐2019) and group B (2022‐2023). Shigella had 0 positive cases in both periods. A notable decline in V parahaemolyticus positivity was observed in the postpandemic period. DEC remained the predominant pathogen in both periods (Figure 2).

The chart illustrates the total number of patients tested (light blue) and the corresponding number of etiologically confirmed positive cases (dark blue) for each study year. The years 2020‐2021 were excluded due to major disruptions in clinical services and surveillance during the peak COVID-19 pandemic period. This exclusion represents an important limitation, as it precludes observation of pathogen trends during the period when infection control measures were most intense.

This single-center retrospective study analyzed clinical and microbiological data from 1064 patients presenting to an infectious diarrhea clinic at a tertiary hospital in Beijing and compared microbial foodborne pathogen detection between the prepandemic (2018‐2019) and postpandemic (2022‐2023) periods. The principal finding was that the overall pathogen positivity rate among tested patients was significantly lower in the postpandemic period (82/503, 16.3%) compared with the prepandemic period (155/561, 27.6%), with V parahaemolyticus and Norovirus showing significant reductions. These findings are consistent with, but do not establish, a temporal association between the COVID-19 pandemic and changes in enteric pathogen detection.

Among the 1064 cases, the predominant demographic comprised individuals aged 16 to 45 years (n=890, 83.6%), with students, civil servants, and retired personnel accounting for 762 (71.6%) cases. This pattern likely reflects the hospital’s location, which is surrounded by academic and research institutions. In terms of clinical characteristics, the study population was predominantly aged 16 to 25 years, with students comprising the largest occupational group. Chen et al [11] similarly reported that individuals testing positive were mainly young and middle-aged adults, highlighting the need for vigilance in monitoring students and other congregate populations.

The proportion of patients aged 26 to 45 and 46 to 65 years differed between group B and group A; however, because group B represents the postpandemic period (2022‐2023) rather than the strict lockdown period, this difference likely reflects a combination of factors, including altered health care–seeking behavior, changes in the clinic’s catchment population, differences in occupational composition, and other unmeasured variables rather than pandemic-related mobility restrictions.

In the etiological analysis, DEC remained the most frequently detected pathogen in both periods (group A: 66/561, 11.8%; group B: 45/503, 9%) [12-14], which is consistent with the findings of Liu et al in Haidian District [15], who reported an 11.8% proportion of DEC. The persistently high detection of DEC may be related to its environmental resilience, low infectious dose, and potential for foodborne transmission through contaminated produce and other food vehicles. The relative stability of Salmonella detection rates between periods (group A: 22/561, 3.9%; group B: 13/503, 2.6%) is consistent with its endemic circulation in animal reservoirs and continuous food supply chain contamination, which may be less affected by personal hygiene measures [16,17].

The significant reduction in V parahaemolyticus detection, from 24/561 (4.3%) to 7/503 (1.4%), is noteworthy [18,19]. This pathogen is classically associated with seafood consumption, particularly raw or undercooked shellfish. The observed decline may reflect changes in food consumption patterns during and after the pandemic, including reduced restaurant dining, increased home cooking, and possible disruptions in seafood supply chains. Additionally, V parahaemolyticus has a summer seasonal peak, and changes in health care–seeking behavior for mild diarrhea during summer months may have contributed to the observed reduction. Norovirus detection also declined significantly, from 43/561 (7.7%) to 17/503 (3.4%) (P=.002), which is biologically plausible given that Norovirus can be transmitted through the fecal-oral route and aerosols; thus, enhanced hand hygiene, mask wearing, and environmental disinfection measures implemented during the pandemic may have reduced its transmission [20,21].

No Shigella cases were identified in either group, which is consistent with the findings of Wang et al [22], who reported a gradual decline in Shigella among foodborne pathogens, and with Lu et al [23], who noted high Norovirus detection rates among viral pathogens and high DEC detection rates among bacterial pathogens. Among cases of foodborne illness, the relative proportions of Salmonella and DEC were higher in group B than in group A, suggesting that these pathogens may require continued surveillance.

It is critical to distinguish between a reduction in detected cases and a true reduction in population-level disease incidence. This hospital-based study cannot establish population-level incidence. The observed lower positivity rate may reflect multiple factors beyond a true decline in disease occurrence, including (1) changes in health care–seeking behavior, whereby patients with milder symptoms may have been less likely to visit the hospital during and after the pandemic; (2) altered health care accessibility and clinic volume; (3) changes in food consumption patterns, including increased home food preparation and reduced dining out; (4) changes in stool sampling practices and clinician testing thresholds; and (5) nonpharmaceutical interventions (hand hygiene, masking, social distancing) that may have genuinely reduced the transmission of enteric pathogens. We are unable to disentangle the relative contributions of these factors in this observational study.

Several additional limitations should be acknowledged. First, this was a single-center study conducted at one infectious diarrhea clinic in a tertiary hospital in Beijing; therefore, the findings may not be representative of the general population or community-level epidemiology in China or in other geographic regions. This study included only symptomatic patients seeking care, which likely excluded milder cases and asymptomatic infections. Second, the exclusion of the 2020‐2021 time period represents a major gap, as this period encompassed the peak of the pandemic, when infection control measures were most intense. This created a discontinuity in temporal trends and meant that we could not characterize changes during this period. Third, we investigated only 5 bacterial and viral pathogens; nonmicrobial foodborne illnesses (chemical contamination, natural toxins, food allergies, and parasites) were not assessed, and thus our results do not represent the full spectrum of foodborne diseases. Fourth, statistical analyses were limited to univariate comparisons, and we were unable to perform multivariate adjustment for all potential confounders. Fifth, the sample size for some individual pathogens was small, limiting statistical power for subgroup comparisons. Finally, we did not have data on total clinic visit volumes to directly quantify changes in health care utilization.

In clinical practice, early management of suspected foodborne cases, particularly those involving DEC and Salmonella, should include appropriate infection control measures, such as hand hygiene, use of masks and gowns, patient education on personal hygiene, environmental disinfection, vital sign monitoring, and dietary guidance. For severe cases, temporary fasting and nutritional support may be required [24,25]. Future efforts should strengthen foodborne disease surveillance through diversified health education channels and coordinated online and offline public awareness campaigns to improve food safety knowledge.

Among patients presenting to a single infectious diarrhea clinic in Beijing, detection rates of bacterial and viral foodborne pathogens were significantly lower in the postpandemic period (2022‐2023) compared with the prepandemic period (2018‐2019), with V parahaemolyticus and Norovirus showing significant declines. These temporal changes may be associated with infection control measures, shifts in health care–seeking behavior, and changes in food consumption patterns; however, this observational study cannot establish causation, and the results do not represent population-level incidence or the full spectrum of foodborne diseases. Continued surveillance and further multicenter studies incorporating longer study periods and molecular subtyping are needed to better understand the long-term implications of the pandemic for foodborne disease epidemiology.